chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
153320870933208710AG43GENIChomozygous980404853
153320882733208828CT45GENIChomozygous980404854
153320920333209204CT32GENIChomozygous980404855
153321053033210531TA40GENIChomozygous980404856
153321053133210532CA41GENIChomozygous980404857
153321218233212183TC42GENIChomozygous980404858
153321263333212634CT69GENIChomozygous980404859
153321344933213450GC12GENIChomozygous980404860
153321387833213879CA10GENIChomozygous980404861
153321412033214121GT73GENIChomozygous980404862
153321433833214339CT64GENIChomozygous980404863
153321468033214681AC27GENIChomozygous980404864
153321479933214800GT13GENIChomozygous980404865
153321514133215142TC42GENIChomozygous980404866
153321551333215514AG44GENIChomozygous980404867
153321552033215521GA44GENIChomozygous980404868
153321570433215705TC45GENIChomozygous980404869
153321582633215827CT27GENIChomozygous980404870
153321586933215870TC27GENIChomozygous980404871
153321598633215987AG18GENIChomozygous980404872
153321605233216053GA22GENIChomozygous980404873
153321614533216146GA19GENIChomozygous980404874
153321620833216209CT20GENIChomozygous980404875
153321676133216762TG53GENIChomozygous980404876